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Article: A peripheral neutrophil-related inflammatory factor predicts a decline in executive function in mild Alzheimer's disease

TitleA peripheral neutrophil-related inflammatory factor predicts a decline in executive function in mild Alzheimer's disease
Authors
KeywordsInflammation
Myeloperoxidase
Interleukin-8
Executive function
Tumor necrosis factor
Memory
Neutrophil gelatinase-associated Lipocalin
Macrophage inflammatory protein-1 beta
Neutrophil
Alzheimer's disease
Issue Date2020
Citation
Journal of Neuroinflammation, 2020, v. 17, n. 1, article no. 84 How to Cite?
Abstract© 2020 The Author(s). Background: Studies suggest a role of the innate immune system, including the activity of neutrophils, in neurodegeneration related to Alzheimer's disease (AD), but prospective cognitive data remain lacking in humans. We aimed to investigate the predictive relationship between neutrophil-associated inflammatory proteins in peripheral blood and changes in memory and executive function over 1 year in patients with AD. Methods: Participants with AD were identified from the Alzheimer's Disease Neuroimaging Initiative (ADNI). Neutrophil gelatinase-associated lipocalin (NGAL), myeloperoxidase (MPO), interleukin-8 (IL-8), macrophage inflammatory protein-1 beta (MIP-1β), and tumor necrosis factor (TNF) were assayed by luminex immunofluorescence multiplex assay at baseline. Confirmatory factor analysis was used to test an underlying neutrophil associated plasma inflammatory factor. Composite z-scores for memory and executive function were generated from multiple tests at baseline and at 1 year. A multiple linear regression model was used to investigate the association of the baseline inflammatory factor with changes in memory and executive function over 1 year. Results: Among AD patients (n = 109, age = 74.8 ± 8.1, 42% women, Mini Mental State Examination [MMSE] = 23.6 ± 1.9), the neutrophil-related inflammatory proteins NGAL (λ = 0.595, p <.001), MPO (λ = 0.575, p <.001), IL-8 (λ = 0.525, p <.001), MIP-1β (λ = 0.411, p =.008), and TNF (λ = 0.475, p <.001) were found to inform an underlying factor. Over 1 year, this inflammatory factor predicted a decline in executive function (β = - 0.152, p = 0.015) but not memory (β = 0.030, p = 0.577) in models controlling for demographics, brain atrophy, white matter hyperintensities, the ApoE ϵ4 allele, concomitant medications, and baseline cognitive performance. Conclusions: An inflammatory factor constructed from five neutrophil-related markers in peripheral blood predicted a decline in executive function over 1 year in people with mild AD.
Persistent Identifierhttp://hdl.handle.net/10722/288799
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBawa, Kritleen K.-
dc.contributor.authorKrance, Saffire H.-
dc.contributor.authorHerrmann, Nathan-
dc.contributor.authorCogo-Moreira, Hugo-
dc.contributor.authorOuk, Michael-
dc.contributor.authorYu, Di-
dc.contributor.authorWu, Che Yuan-
dc.contributor.authorBlack, Sandra E.-
dc.contributor.authorLanctôt, Krista L.-
dc.contributor.authorSwardfager, Walter-
dc.date.accessioned2020-10-12T08:05:54Z-
dc.date.available2020-10-12T08:05:54Z-
dc.date.issued2020-
dc.identifier.citationJournal of Neuroinflammation, 2020, v. 17, n. 1, article no. 84-
dc.identifier.urihttp://hdl.handle.net/10722/288799-
dc.description.abstract© 2020 The Author(s). Background: Studies suggest a role of the innate immune system, including the activity of neutrophils, in neurodegeneration related to Alzheimer's disease (AD), but prospective cognitive data remain lacking in humans. We aimed to investigate the predictive relationship between neutrophil-associated inflammatory proteins in peripheral blood and changes in memory and executive function over 1 year in patients with AD. Methods: Participants with AD were identified from the Alzheimer's Disease Neuroimaging Initiative (ADNI). Neutrophil gelatinase-associated lipocalin (NGAL), myeloperoxidase (MPO), interleukin-8 (IL-8), macrophage inflammatory protein-1 beta (MIP-1β), and tumor necrosis factor (TNF) were assayed by luminex immunofluorescence multiplex assay at baseline. Confirmatory factor analysis was used to test an underlying neutrophil associated plasma inflammatory factor. Composite z-scores for memory and executive function were generated from multiple tests at baseline and at 1 year. A multiple linear regression model was used to investigate the association of the baseline inflammatory factor with changes in memory and executive function over 1 year. Results: Among AD patients (n = 109, age = 74.8 ± 8.1, 42% women, Mini Mental State Examination [MMSE] = 23.6 ± 1.9), the neutrophil-related inflammatory proteins NGAL (λ = 0.595, p <.001), MPO (λ = 0.575, p <.001), IL-8 (λ = 0.525, p <.001), MIP-1β (λ = 0.411, p =.008), and TNF (λ = 0.475, p <.001) were found to inform an underlying factor. Over 1 year, this inflammatory factor predicted a decline in executive function (β = - 0.152, p = 0.015) but not memory (β = 0.030, p = 0.577) in models controlling for demographics, brain atrophy, white matter hyperintensities, the ApoE ϵ4 allele, concomitant medications, and baseline cognitive performance. Conclusions: An inflammatory factor constructed from five neutrophil-related markers in peripheral blood predicted a decline in executive function over 1 year in people with mild AD.-
dc.languageeng-
dc.relation.ispartofJournal of Neuroinflammation-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectInflammation-
dc.subjectMyeloperoxidase-
dc.subjectInterleukin-8-
dc.subjectExecutive function-
dc.subjectTumor necrosis factor-
dc.subjectMemory-
dc.subjectNeutrophil gelatinase-associated Lipocalin-
dc.subjectMacrophage inflammatory protein-1 beta-
dc.subjectNeutrophil-
dc.subjectAlzheimer's disease-
dc.titleA peripheral neutrophil-related inflammatory factor predicts a decline in executive function in mild Alzheimer's disease-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s12974-020-01750-3-
dc.identifier.pmid32171317-
dc.identifier.pmcidPMC7071641-
dc.identifier.scopuseid_2-s2.0-85081748561-
dc.identifier.volume17-
dc.identifier.issue1-
dc.identifier.spagearticle no. 84-
dc.identifier.epagearticle no. 84-
dc.identifier.eissn1742-2094-
dc.identifier.isiWOS:000520972700002-
dc.identifier.issnl1742-2094-

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